Highly elastomeric and paintable silicone compositions

ABSTRACT

Highly elastomeric, curable, paintable silicone compositions are provided. The paintable silicone compositions comprise an organopolysiloxane, a silicone functional crosslinker, and an organic polymer. The highly elastomeric, curable, paintable silicone compositions have an elongation of at least 150% and are useful as paintable sealants and caulks.

FIELD OF THE INVENTION

The present invention relates to a unique family of one and twocomponent highly elastomeric vulcanizable paintable silicone sealantsand extrusions exhibiting high elongation characteristics combined withexcellent adhesion and weathering resistance. They can be designed tohave a wide range of properties ranging from low modulus to highstrength self-adhering curable room temperature vuclanizable (RTV)silicone compositions exhibiting superior paintability and adhesioncharacteristics while maintaining the outstanding weathering resistanceof silicone elastomers.

BACKGROUND OF THE INVENTION

Silicone compositions are widely used in the construction industry aswell as other industrial applications, such as automotive, electronics,aerospace and consumer markets because these materials possessself-bonding adhesion properties to several types of substrates such asglass, metal, ceramics, fabrics, wood, leather, plastics and paper. Inaddition, superior properties such as low temperature flexibility,high-temperature stability, good electrical insulation and resistance tochemicals and UV resistance are inherent in silicone-based products.Thus, silicone extrusions are widely used in a variety of applications.A disadvantage of cured silicone compositions, however, is that they areconsidered to be unpaintable. The low surface energy of the siliconeprevents latex or oil based paints to wet the surface of the curedsilicone. The paint tend to shrink away from the silicone surfaceleaving a poor surface appearance commonly referred to in the industryas “fish eyes.”

Attempts to improve paintability of silicone compounds have been made byadding inorganic fillers to the uncured silicone. For example, siliconesealants have been formulated with the addition of acicular, i.e.needle-like, calcium carbonate to the polyorganosiloxane. In suchsealants, the acicular particles become oriented on the surface of thesealant during curing. The surface of the cured sealant has improvedpaintability, but the addition of the acicular calcium carbonate resultsin other problems such as low elasticity. The generally high loading ofcalcium carbonate necessary to achieve improved paintabilitydeleteriously affects the elasticity of the silicone sealant such thatits tensile elongation is lower than desired.

Plasticizer can be added to counter the negative effect of calciumcarbonate on the extensibility of the silicone. However, plasticizersdetract from the paintability of the silicone sealant.

It is desirable to provide a curable silicone composition that, oncecured, is paintable by many types of coatings. It is also desirable toprovide silicone extrusions, sealants, adhesives, and caulks that arepaintable over an extended period of time and which maintain theexcellent elastomeric and other properties inherent in silicone.

SUMMARY OF THE INVENTION

The organopolysiloxane compositions of the present invention comprise anorganic polymer, an organic oligomer, or combinations of an organicpolymer and an organic oligomer; an organopolysiloxane polymer; and acrosslinker. The compositions may further comprise other additives tomodify the properties of the organopolysiloxanes. The organic polymercan be a homopolymer, a copolymer and mixtures thereof having reactiveor non-reactive terminal groups. It has been discovered that suchcompositions, when cured, produce a silicone sealant that exhibitsexcellent paintability and superior weathering properties.

The silicone compositions of the present invention, once cured, can bepainted without the formation of “fish eyes” on the painted surface, andhas an elongation of at least 150%. The elongation of the cured siliconecomposition may be 200% or greater, 800% or greater, or even 1000% orgreater.

The curable silicone compositions of the present invention generallycontain from about 50% to about 95% (by weight, based on total polymer)organopolysiloxane polymer; from about 1% to about 10% (by weight, basedon organopolysiloxane) silicone functional crosslinker; and from about5% to about 50% (by weight, based on total polymer) dispersed organicpolymer. Preferably, the curable silicone compositions comprise from 55%to 93% by weight organopolysiloxane polymer. More preferably, thecurable silicone compositions comprise from 57% to 91% by weightorganopolysiloxane polymer.

Preferably, the curable silicone compositions of the present inventioncomprise from 7% to 45% by weight organic polymer. More preferably, thecurable silicone compositions comprise from 9% to 43% by weight organicpolymer.

The organopolysiloxane polymers preferably have at least two reactivefunctional groups on the polymer chain. The reactive functional groupsmay be from hydroxyl, alkoxy, silicone alkoxy, acyloxy, ketoximo, amino,amido, aminoxy, alkenoxy, alkenyl, enoxy and mixtures thereof. Thereactive functional groups are end groups, pendant groups, or acombination thereof.

The organic polymer used in the curable silicone compositions of thepresent invention may be selected silylated and non-silylatedpolyurethanes, silylated allylic terminated polyethers, polyetherscontaining one or more silicone functional groups, silylated andnon-silylated acrylic functional polymers, silylated and non-silylatedbutyl functional polymers, and copolymers and mixtures thereof.

The amount of organic polymer used in preparing the paintable, curablesilicone compositions of the present invention depends on the organicpolymer used. The organic polymer is added by weight, based on totalpolymer, and ranges from about 15% to about 50% for silylated andnon-silylated polyurethane; from about 15% to about 50% for silylatedallylic terminated polyether; from about 15% to about 50% silylatedallylic terminated acrylic polyether; from about 15% to about 50% forpolyether having a silicone functional group; from about 10% to about50% for silylated and non-silylated acrylic multipolymer; and from about5% to about 50% for silylated and non-silylated butyl functionalpolymer.

The organopolysiloxane used in the present invention preferably has amolecular weight in the range from 20,000 to 100,000 grams/mole. Theorganopolysiloxane has at least two reactive groups and an organicpolymer selected from the group consisting of silylated polyurethane,non-silylated polyurethane, silylated allylic terminated polyether, apolyether that contains a silicone functional group, a silylated acrylicfunctional polymer, a non-silylated acrylic functional polymer, asilylated butyl functional polymer, a non-silylated butyl functionalpolymer, and mixtures thereof. The reactive groups may be selected fromend groups, pendant groups, and combinations thereof.

The silicone crosslinker used in the paintable, curable siliconecompositions of the present invention may be selected from suchcrosslinkers as oximes, alkoxysilanes, epoxyalkylalkoxysilanes, amidosilanes, aminosilanes, enoxysilanes, tetraethoxysilanes,methyltrimethoxysilane, vinyltrimethoxysilane,glycidoxypropyltrimethoxsilane, vinyltris-isopropenoxysilane,methyltris-isopropenoxysilane, methyltris-cyclohexylaminosilane,methyltris-secondarybutylaminosilane, condensation cure catalysts, andcombinations thereof. Preferred oxime crosslinkers includevinyltrismethylethylketoximosilane, methyltrismethylethylketoximosilane,and combinations thereof.

In accordance with the present invention, the paintable, curablesilicone compositions may be 1-part curable compositions or 2-partcurable compositions. The paintable, curable silicone composition may beeither thermally curing systems and room temperature curing systems. Thepaintable, curable silicone may be an extrusion or in situ curedsystems.

The paintable, curable silicone compositions of the present inventionmay further comprise from about 0.01% to about 2% (by total weight)catalyst. Suitable catalysts include metal salts of carboxylic acids,organotitanates, platinum complexes, peroxides, and combinationsthereof. Preferred catalysts comprising metal salts of carboxylic acidsinclude dibutyltindilaurate, dibutyltindiacetate,dimethyltindi-2-ethylhexanoate, and combinations thereof. Preferredorganotitanates include tetrabutyltitanate, tetra-n-propyltitanate,diisopropoxydi(ethoxyacetoacetyl)titanate,bis(acetylacetonyl)diisopropyl titanate and combinations thereof.

The paintable, curable silicone composition may further include fromabout 3% to about 60% (by total weight) reinforcement agents,semi-reinforcing agents, or combinations thereof. Some preferredreinforcement agents include hydrophobic treated fumed silicas,untreated fumed silicas, hydrophobic precipitated calcium carbonates,ground calcium carbonates, talc, zinc oxides, polyvinyl chloridepowders, soft acrylic polymers and combinations thereof. The paintable,curable silicone compostions may further comprise from about 0.5% toabout 2% (by total weight) adhesion promoter.

A preferred organic polymer used in the paintable, curable siliconecompositions is a silylated polyurethane polymer. This silylatedpolyurethane polymer may be derived by the steps of a) reacting adiisocyanate compound with a polyol to form an intermediate, wherein theintermediate is selected from isocyantates or hydroxyl terminatedpolyurethane prepolymers; and b) silylating the intermediate.Preferably, the intermediate is silylated with an organo functionalsilane having one or more hydrolyzable groups. Some preferredhydrolyzable groups include

(OCH₃)₃, (OCH₂CH₃)₃, oximo, enoxy, isopropenoxy,and combinations thereof.

Preferably, the organo functional silane is of the formula:R″—X—Si—R′wherein R′ is selected from the group consisting of (OCH₃)₃, (OCH₂CH₃)₃,CH₃(OCH₃)₂, or CH₃(OCH₂CH₃)₂, other hydrolyzable groups such as oximosubstituents, enoxy, and isopropenoxy; R″ is selected from the groupconsisting of amino, ureido, mercapto, isocyanato, and epoxy; and X isC₁ to C₈. The molecular weight of the polyurethane prepolymerintermediate ranges from 5,000 to 50,000 g/mol. The polyurethaneprepolymer intermediate has a NCO:OH ratio in the range from 1.4:1 to3:1 or an OH:NCO ratio in the range from 1.4:1 to 3:1.

The organic polymer may also be silylated allylic terminated polyether;wherein the silylated allylic terminated polyether is derived from thereaction of a vinyl alkyl terminated polyol with a hydride functionalsilane. Preferably, the hydride functional silane is selected from thegroup consisting of triethoxysilane, trimethoxysilane,methyldiethoxysilane, methyldimethylsilane and combinations thereof.

The organic polymer may also be a polyether having a silicone functionalgroup. Preferably, when the organic polymer is a polyether having asilicone functional group, the silicone functional group is ahydrolyzable silane group. Preferable polyethers having a siliconefunctional group are those having a molecular weight in the range fromabout 2,000 to about 50,000 g/mole.

The present invention also relates to the methods of making such curablesilicone sealant compositions.

DETAILED DESCRIPTION OF THE INVENTION

The organopolysiloxane compositions of the present invention arecomprised of a reactive organopolysiloxane polymer, a polymer phasecomprising an organic polymer/oligomer having limited compatibility withthe reactive organopolysiloxane polymer and a silicone functionalcross-linking system. The organic polymer/oligomer phase may containreactive organosilyl terminal groups which can enter into avulcanization reaction with the silicone functional crosslinking systemattached to the reactive organopolysiloxane polymer. To maintain thesuperior weathering resistance of typical elastomeric silicones andexcellent paintability unlike normal silicone elastomers, theconcentration of the organic polymer/oligomer must be maintained withinprecise ranges. Both elevated and depressed levels of the organicpolymer/oligomer phase will cause a loss of good paintability. Theoutstanding weathering resistance of these compositions has beendemonstrated by the lack of surface degradation after more than 20,000hours exposure in a Xenon Arc Weatherometer as discussed below. Thecompositions of the present invention may be painted by a variety ofpaints, even after curing for several weeks while maintaining theexcellent elastomeric properties inherent in silicone.

As used herein, the phrase “semi-compatible organic polymer/oligomer”encompasses organic polymers and oligomers that are not fully compatiblewith the organopolysiloxanes used in the present invention, i.e., thesemi-compatible organic polymers/oligomers are not fully miscible withthe organopolysiloxanes of the present invention.

The paintable silicone composition of the present invention is generallymade by blending a semi-compatible organic polymer/oligomer, across-linker, and other additives generally used in silicone sealantsand extrusions in the presence of a reactive polysiloxane fluid.

The curable organopolysiloxane composition of the present inventioncomprises a reactive organopolysiloxane polymer, a semi-compatibleorganic polymer/oligomer, a crosslinker, and optionally may include anadhesion promoter, a reinforcement agent, a rheology modifier, a chainextender, and so forth. Once the composition is reacted, the resultingsilicone sealant is paintable even after having been cured for aprolonged period.

The curable organopolysiloxane composition comprises by weight fromabout 5% to about 50%, preferably from about 7% to about 45%, and evenmore preferably from about 9% to about 43% organic polymer/oligomer,from about 50% to about 95%, preferably from about 55% to about 93%,even more preferably from about 57% to about 91% organopolysiloxanepolymer. When cured, the paintable silicone composition has anelongation of at least 150%, and up to 200%, 400%, and even greater than800%. The paintable silicone compositions described herein have beenshown to have elongations of greater than 1000%.

The polyorganosiloxane generally contains at least two reactivefunctional groups on the polymer chain, preferably at the terminalportion thereof, i.e., preferably the reactive functional groups areend-groups. The polyorgansiloxanes useful in this invention are thosewhich contain a condensable functional group which can be an hydroxylgroup, or hydrolyzable group such as a silicon-bonded alkoxy group,acyloxy group, ketoximo group, amino group, amido group, aminoxy group,an alkenoxy group, and so forth.

The organopolysiloxane polymer is of the formula:

where R¹ and R², independently, are an alkyl having from 1 to 8 carbonatoms, desirably from 1 to 4 carbon atoms with methyl being preferred,or is an aromatic group or substituted aromatic group having from 6 to10 carbon atoms with phenyl being preferred, and “n” is such that theweight average molecular weight of the organopolysiloxane is from about10,000 to about 200,000 and desirably from about 20,000 to about 100,000grams/mole. It is to be understood that the above polymers also contain,as noted above, two or more reactive functional groups (X) therein. Thefunctional groups, independently, can be OH, or OR³, or N(R⁴)₂, enoxy,acyloxy, oximo, or aminoxy, wherein these functional groups may havesubstituents at any substitutable location. For example,

wherein R³ through R¹⁴ are, independently, an alkyl or cycloalkyl havingfrom about 1 to about 8 carbon atoms.

The organopolysiloxane of the present invention may be depicted as

The one or more R groups, independently, is an alkyl having from 1 to 8carbon atoms or an aromatic or an alkyl-aromatic having from 6 to 20carbon atoms and optionally containing one or more functional groupsthereon, such as amine, hydroxyl, alkene, alkoxy, and so forth. Theamount of the functional groups, i.e., m, is 1, 2 or 3.

The reactive functional group (X), can be OH, or OR′, or N(R′), orenoxy, or acyloxy, or oximo, or aminoxy, or amido, wherein the reactivefunctional group may have substitutions, R′, at any substitutable C orN, and which is selected from the group consisting of an alkyl havingfrom about 1 to about 8 carbon atoms, an aromatic, an alkyl-aromatichaving from 6 to 20 carbon atoms, and wherein R′ may optionally containone or more functional groups thereon such as amine, hydroxyl, and soforth. An organopolysiloxane fluid can furthermore contain a blend oftwo or more different polysiloxanes and/or organopolysiloxanes havingdifferent molecular weights. The polysiloxanes are generally a viscousliquid and are commercially available from several siliconemanufacturers such as Wacker Corporation, General Electric, Dow Corningand Rhone-Poulenc.

The paintable sealant compositions of the present invention are cured bygenerally subjecting them to moisture or a curative. Either aconventional one-component or two-component cure system can be utilized.In a conventional one-component cure, the organopolysiloxane isconverted to a compound having an alkoxy, an oxime, an enoxy, an amido,an amino, or an acetoxy blocking group in a manner well known to the artand to the literature. Conventional condensation catalysts may beutilized, such as an organotin, for example, dibutyltindilaurate,dibutyltindiacetate, dimethyltindi-2-ethylhexanoate, ordimethylhydroxytinoleate, or an organotitanate.

The semi-compatible organic polymers/oligomers used in accordance withthe present invention are generally organic polymers included in any ofa variety of well known polymers having non-reactive or reactivefunctional groups, or polymers with no functional groups, and which canbe intermixed with reactive organopolysiloxane polymer. The organicpolymer can be a homopolymer, a copolymer or mixtures thereof and thepolymer can be a crosslinking or a non-crosslinking polymer. Organicpolymers include aromatic and aliphatic polyurethanes, polyurea,polyether, polyester, acrylic, polystyrene, styrene butadiene,polybutadiene, butyl rubber, with or without other organo functionalgroups attached to then, and mixtures thereof. Aromatic and aliphaticpolyurethanes may have different backbones such as polyester, polyether,polyacrylate, polybutadiene, polycarbonate, and so forth, or acombination thereof. Futhermore, they could also have other functionalgroups, such as acrylates, amides, maleic anhydride, and so forth.

Another suitable organic polymer is a reactive silylated aromatic oraliphatic polyurethane polymer from the above general polyurethanecategory. Polyurethane prepolymers whose terminal ends are partially, orfully, end-capped with either silane groups or with a combination ofsilane groups and end capping groups that have been derived from one ormore aromatic alcohols, or one or more aliphatic alcohols, or acombination of one or more aromatic alcohols and one or more aliphaticalcohols.

Examples of suitable silanes corresponding to the above-mentioned systeminclude N-phenylaminopropyltrimethoxysilane,N-ethylaminoisobutyltrimethoxysilane, γ-aminopropyltrimethoxysilane,γ-aminopropyltriethoxysilane, and the reaction product of an aminosilane(such as γ-aminopropyltrimethoxysilane, γ-aminopropyltriexthoxysilane,γ-aminopropylmethyldimethoxysilane) with an acrylic monomer (such asethyl acrylate, 2-ethylhexyl acrylate, methyl acrylate, methylmethacrylate, and glycidal acrylate), mercaptosilane, the reactionproduct of a mercaptosilane with a monoepoxide, the reaction product ofan epoxysilane with a secondary amine, isocyanato propyl triethoxysilane, and ureido propyl trimethoxy silane.

In another embodiment of the invention the organic polymer is asilylated allylic terminated linear or branched polyether. The polyetherbackbone may have other functional groups, such as acrylates, amides,maleic anhydride, and so forth. The polymers' terminal ends could bepartially or fully end-capped either with silane groups or with acombination of silane groups and other end-capping groups.

Another suitable class of organic polymer/oligomer are reactivesilylated polyols. These polyols may be selected from polyester,polyether, polyacrylate, polybutadiene, polycarbonate, and so forth. Thesilylation may be done as discussed above.

Optionally, the blocked one-component cure system can containcrosslinking agents as set forth herein. In a two-component cure system,crosslinking agents, such as a multi-functional alkoxy silane oroligomers thereof and catalysts are kept separate from theorganopolysiloxane until reaction. The amount of catalyst for thetwo-component system is generally higher than in the one-componentsystem. Such cure systems are well known to the art, see, e.g., MauriceMorton, et al., Rubber Technology, 3^(rd) Ed., pp. 406-407, (1987),which is hereby fully incorporated by reference. When a two part cure isused, the two-part cure may either be a room-temperature curable or athermally curing material.

While a variety of conventional crosslinkers are suitable, oxime andalkoxy crosslinkers are preferred, such as, for example,vinyltris-methylethylketoximosilane, andmethyltris-methylethylketoximosilane, and alkoxysilanes such asmethyltrimethoxysilane and vinyltrimethoxysilane. Methyltrimethoxysilaneis available, for example, under the trade name A-1630 andvinyltrimethoxysilane is available, for example, under the trade nameA-171 from General Electric-OSI Specialties.Methyltris-methylethylketoximosilane (MOS) is available under the tradename OS-1000, for example, and vinyl tris-methylketoximosilane under thetrade name of OS-2000 by Honeywell Corporation, for example. Othercrosslinkers are also suitable, such as alkoxysilanes,epoxyalkylalkoxysilanes, amidosilanes, aminosilanes, enoxysilanes andthe like, as well as tetraethoxysilanes, glycidoxypropyltrimethoxsilane,vinyltris-isopropenoxysilane, methyltris-isopropenoxysilane,methyltris-cyclohexylaminosilane, andmethyltris-secondarybutylaminosilane. Mixtures of crosslinkers may alsobe employed. The amount of the crosslinking agent is generally fromabout 0.2 to about 20 parts by weight, desirably from about 1 to about10 parts by weight, and preferably from about 1.5 to about 6.5 parts byweight for every 100 parts by weight of saidcopolymer-organopolysiloxane. Addition cure crosslinkers may also beused in conjunction with alkenyl functional organopolysiloxane polymers.These crosslinkers may be pre-reacted to the polyorganosilane polymers.

The crosslinker is used in amounts which are conventionally used formaking curable silicone elastomeric compositions. Those skilled in theart may determine the proper amounts for room-temperature curable andthermally curable crosslinkers. The amounts used will vary dependingupon the particular crosslinker chosen and the properties of the curedelastomer desired, and may readily be determined by those of ordinaryskill in the art.

A mixture of polyorganosiloxane and crosslinker will usually cure atroom temperature when exposed to moisture, however, sometimes it isdesirable to accelerate the cure rate, i.e., reduce the time to curecomposition. In these situations a catalyst may be used. Preferredcatalysts include metal salts of carboxylic acids such asdibutyltindilaurate, dibutyltindiacetate, anddimethyltindi-2-ethylhexanoate; organotitanates such astetrabutyltitanate, tetra-n-propyltitanate,diisopropoxydi(ethoxyacetoacetyl)titanate, andbis(acetylacetonyl)diisopropyltitanate. Alternatively, thermally curablematerials may be used in addition to or in place of the room-temperaturecurable systems.

The paintable sealant compositions described herein become tack free ingenerally about 0.05 to about 12 hours, desirably from about 0.1 toabout 2 hours once the cure is initiated. The sealants becomesubstantially cured, i.e., chemically crosslinked, in about 7 days,although this may vary depending upon the curing system, depth of cure,and particularly the catalyst employed. The sealants are typicallycompletely cured at about 21 days at 25° C. and 50% relative humidity.However, in the case of extruded materials, they would be vulcanized asthey come out from the extruder.

The curable silicone compositions described herein may be made to pass a“paint adhesion tape test.” In accordance with this specification, the“paint adhesion tape test” is set forth as ASTM test method D3359 and isperformed as follows. The sealant composition is adhered to a surfaceand painted. A crisscross, i.e., cross-hatches, are cut through thepaint and sealant layers using a razor blade. A 0.5-inch wide by 4-inchlong strip of clear Scotch® brand adhesive tape (3M Corp.) is firmlyapplied across the pre-cut crisscross area. The tape, which istenaciously adhered to the painted surface, is then pulled away at a 90°angle. If the paint remains intact on the surface of the sealant it isconsidered to have passed the test.

Optionally, an adhesion promoter may be added to the paintable sealant.The amount of adhesion promoter may readily be determined by those ofordinary skill in the art. The amount of the adhesion promoter in thepaintable sealant is generally from 0 to about 10, desirably from about1 to about 8, preferably from about 2 to about 6, and more preferablyfrom about 1.5 to about 3 parts by weight per 100 parts oforganosilicone polymer.

The adhesion promoter, although optional, is highly preferred; theadhesion promoter provides the sealant with long-term adhesion to thesubstrate. Suitable classes of adhesion promoters are aminoalkyl,mercaptoalkyl, ureidoalkyl, carboxy, acrylate and isocyanuratefunctional silanes. Examples of suitable adhesion promoters aremercaptopropyltrimethoxysilane, glycidoxypropyltrimemethoxysilane,aminopropyltriethoxysilane, aminopropyltrimethoxysilane,aminoethylaminopropyltrimethoxysilane, ureidopropyltrimethyloxysilane,bis-γ-trimethoxysilylpropylurea,1,3,5-tris-γ-trimethyloxysilylproplisocyanurate,bis-γ-trimethoxysilylpropylmaleate and fumarate andγ-methacryloxypropyltrimethoxysilane.

Optionally, reinforcing agents may be added to the paintable sealantcompositions of the present invention. The amount of the reinforcingagent is generally from 0 to about 250, desirably from about 30 to about200, preferably from about 20 to about 150, and more preferably fromabout 10 to about 100 parts by weight of polymer.

The reinforcing agents are optional, although highly preferred,particularly when the sealant is used as a caulk. Reinforcing agentsincrease tensile strength in the cured sealant and reduce sag of theuncured sealant. The reinforcing agent also functions as a thixotrope.Such reinforcing agents are finely divided particulates and include boththe conventionally known reinforcing agents and semi-reinforcing agents,typically having a particle size less than about 10 microns, preferablyabout 5 microns or less, more preferably about 0.1 microns or less.Suitable reinforcing agents include hydrophobic treated fumed silicas,such as TS 720 from Cabot Corporation, or R-972 from DegussaCorporation, hydrophobic precipitated calcium carbonates, talc, zincoxides, polyvinyl chloride powders, and soft acrylates such as those ofU.S. Pat. No. 6,403,711B1, incorporated herein by reference. Otheringredients can also be utilized in the sealant formulation in amountsup to about 20 parts by weight and desirably from about 0.01 to about 15parts by weight per 100 parts by weight of the copolymer and theorganopolysiloxane. Such ingredients include fungicides. Moreover,extender fillers such as ground calcium carbonates and diatomaceousearth are optionally employed. Such extenders have minimal or noreinforcing effect and/or minimal or no thixotropic effect.

UV stabilizers may also optionally be added. Pigments or colorants suchas titanium dioxide, iron oxide, carbon black are optionally employed toimpart color to the sealant and/or to act as ultraviolet stabilizer. LTVinhibitors, anitozonates are also optionally added.

The sealant in its uncured state may optionally contain solvents such asorganic solvents to reduce the viscosity.

EXAMPLES Example 1

In this example, about 43% organic polymer (based on the total weight oforganic and inorganic polymer) was used to prepare a medium modulussealant with a shore-A of 15. The organic polymer comprised a silylterminated polyurethane. The amounts are listed in Table 1 below. TABLE1 Weight Composition Percent   2400 cps. silanol terminateddimethylpolysiloxane 10.44 50,000 cps. silanol terminateddimethylpolysiloxane polymer 23.43 Soft acrylic filler (thixotrope)19.38 Hydrophobic treated precipitated calcium carbonate 5.86Hexamethyldisilazane 0.35 Hydrophobic treated ground calcium carbonate2.34 Acrylic functional plasticizer 7.14 Dimethylbis-secondarybutylaminosilane 0.64 Methyltris-methylethylketoximosilane 3.99 Atrimethoxysilylalkyl terminated polyurethane 25.56Aminoethylaminopropyltrimethoxysilane 0.86 Dibutyltindilaurate 0.01TOTAL 100.00

The above composition was painted after curing, yielding a smoothpainted surface having no “fish eyes.” The above composition passed thepaint adhesion test, as described in the specification. This compositionalso maintained excellent weatherability as demonstrated with no surfacecracks and no change in shore-A, even after more than 20,000 hours of UVexposure in the Xenon weatherometer.

Example 2

In this example, about 29% (by weight, based on total polymer) organicpolymer was used to prepare a medium modulus sealant with a shore-A of15. The organic polymer comprised a silyl terminated polyether polymeras shown in Table 2. This composition was designed to give a paintablefast curing silicone sealant having medium modulus properties combinedwith excellent adhesion properties on plastics, glass and anodizedaluminum. TABLE 2 Weight Composition Percent 50,000 cps. silanolterminated dimethylpolysiloxane polymer 25.46 20,000 cps. silanolterminated dimethylpolysiloxane polymer 16.97 Hydrophobic treatedprecipitated calcium carbonate 33.94 Hexamethyldisilazane 0.85Dimethylbis-secondary butylaminosilane 2.25Vinyitris-methylethylketoximosilane 1.70 Alkoxy silyl terminatedpolyether 16.97 Aminoethylaminopropyltrimethoxysilane 1.80Dibutyltindiacetate 0.06 TOTAL 100.00

The unpainted composition upon curing had a tack free of time of 15minutes accompanied by tooling time of 9 minutes. It underwent more than20,000 hours of weathering tests in the Xenon Arc Weatherometer withoutany observable surface changes taking place. The sealant had excellentpaintability. Laboratory studies indicated that the sealant retained itspaintability characteristics indefinitely as shown by periodicpaintability tests carried over a period of 79 days. The paintedcomposition was smooth and had no “fish eyes.”

Example 3

In this example, about 24% (by weight, based on total polymer) organicpolymer was used to prepare a medium modulus sealant. The organicpolymer comprised a silyl terminated polyether polymer as shown in Table3, below. TABLE 3 Weight Composition Percent 50,000 cps. silanolterminated dimethylpolysiloxane polymer 3.83 20,000 cps. silanolterminated dimethylpolysiloxane polymer 34.51   2400 cps. silanolterminated dimethylpolysiloxane polymer 4.02Vinyltris-methylethylketoximosilane 1.53Dimethylbis-secondarybutylaminosilane 2.037 Hexamethyldisilazane 0.84Hydrophobic treated precipitated calcium carbonate 30.68 Soft acrylicfiller 7.48 Alkoxy silyl terminated polyether polymer 13.42Aminopropyltriethoxysilane 1.63 Dibutyltindiacetate 0.023 TOTAL 100.00

The above composition was painted after curing, yielding a smoothpainted surface having no “fish eyes.” The above composition also passedthe paint adhesion test while maintaining excellent weatherability asdemonstrated with no surface cracks and no change in shore-A, even aftermore than 20,000 hours of UV exposure in the Xenon weatherometer.

Example 4

In this example, about 26% (by weight, based on total polymer) organicpolymer was used to prepare a medium modulus sealant. The organicpolymer comprised an MDI terminated polyurethane polymer as shown inTable 4, below. TABLE 4 Weight Composition Percent 50,000 cps. silanolterminated dimethylpolysiloxane polymer 26.12 20,000 cps. silanolterminated dimethylpolysiloxane polymer 17.41Vinyltris-methylethylketoximosilane 2.394Dimethylbis-secondarybutylaminosilane 1.22 Hexamethyldisilazane 0.871Hydrophobic treated precipitated calcium carbonate 34.83 MDI terminatedpolyurethane prepolymer 15.24 Aminopropyltriethoxysilane 1.85Dibutyltindiacetate 0.065 TOTAL 100.00

The above composition was painted after curing, yielding a smoothpainted surface having no “fish eyes.” The above composition also passedthe paint adhesion test while maintaining excellent weatherability asdemonstrated with no surface cracks after UV exposure of more than20,000 hours in the Xenon Weatherometer.

Example 5

In this example, about 31% (by weight, based on total polymer) organicoligomer was used to prepare a silicone sealant. The organic oligomercomprised an oximo silane terminated polyether polyol as shown in Table5, below. The oximo silane terminated polyether polyol was prepared byprereacting it with vinyl-methylethylketoximosilane. TABLE 5 WeightComposition Percent 50,000 cps. silanol terminated dimethylpolysiloxanepolymer 24.90 20,000 cps. silanol terminated dimethylpolysiloxanepolymer 16.60 Vinyltris-methylethylketoximosilane 2.90 Oximo silaneterminated polyether polyol 17.43 Dimethylbis-secondarybutylaminosilane2.20 Hexamethyldisilazane 0.95 Hydrophobic treated precipitated calciumcarbonate 33.20 Aminopropyltriethoxysilane 1.76 Dibutyltindiacetate 0.06Total 100.00

The above composition was painted after curing, yielding a smoothpainted surface having no “fish eyes.” The above composition also passedthe paint adhesion test while maintaining excellent weatherability asdemonstrated with no surface cracks and no change in shore-A, even aftermore than 20,000 hours of UV exposure in the Xenon weatherometer.

Example 6

In this example, about 15% (by weight, based on total polymer) organicpolymer was used to prepare a paintable sealant. The sealant had aShore-A Hardness of 40, accompanied by an elongation of 760% and tensilestrength of 220 psi. The organic polymer comprised an acrylic terpolymerand polyether polyol as shown in Table 6, below. TABLE 6 WeightComposition Percent 50,000 cps. silanol terminated dimethylpolysiloxanepolymer 24.42 20,000 cps. silanol terminated dimethylpolysiloxanepolymer 16.28 Hydrophobic precipitated calcium carbonate 32.56 Groundcalcium carbonate 7.79 Talc 0.90 Titanium dioxide 0.26Hexamethyldisilazane 0.81 Dimethylbis-secondarybutylaminosilane 2.16Vinyltris-methylethylketoximosilane 1.63 Ethyl acrylate acrylonitrileacrylic acid terpolymer 6.81 Polyether polyol 0.20 Butyl benzylphthalate 0.77 Solvent 2.77 Ceramic fiber 0.85Aminoethylaminopropyltrimethoxysilane 1.73 Dibutyltindiacetate 0.06Total 100.00

After curing, the above sealant was painted with acrylic latex paint.The painted surface was smooth, and showed no fish eyes. Three daysafter painting, the surface was subjected to the paint adhesion test,described above without any paint removal taking place.

Example 7

In this example, about 9% (by weight, based on total polymer weight)organic polymer was used to prepare a paintable sealant. It had aShore-A Hardness of 43, accompanied by an elongation of 355% and atensile strength of 300 psi. The organic polymer comprised anisobutylene-isoprene copolymer and polybutene and a hydrocarbon resintackifier as shown in Table 7, below. TABLE 7 Weight Composition Percent50,000 cps. silanol terminated polydimethylsiloxane polymer 24.42 20,000cps. silanol terminated polydimethylsiloxane polymer 16.28 Hydrophobicprecipitated calcium carbonate 32.56 Ground calcium carbonate 11.14Titanium dioxide 0.27 Magnesium carbonate 0.22 Crystalline silica 0.09Hexamethyldisilazane 0.81 Dimethylbis-secondarybutylaminosilane 2.16Vinyltris-methylethylketoximosilane 1.63 Polybutene 2.81 Isobutyleneisoprene copolymer 1.14 Hydrocarbon resin 0.24 Castor oil 0.24 Solvent2.89 Aminoethylaminopropyltrimethoxysilane 1.73 Dibutyltindiacetate 0.06Total 100.00

The resulting sealant was painted and tested in the same manner asdescribed earlier. The painted surface was smooth and had no fish eyes.The above composition also passed the paint adhesion test whilemaintaining excellent weatherability as demonstrated with no surfacecracks and no change in shore-A.

The examples included herein are for illustration and are not meant tolimit the scope of the invention.

1. A curable silicone composition comprising: organopolysiloxane,silicone functional crosslinker; and organic polymer; wherein thecurable silicone composition, once cured, can be painted without fisheyes; and wherein the curable silicone composition, once cured, has anelongation of at least 150%.
 2. The curable silicone composition ofclaim 1 wherein the curable silicone composition, once cured has anelongation of at least 200%.
 3. The curable silicone composition ofclaim 2 wherein the curable silicone composition, once cured, has anelongation of at least 800%.
 4. A curable silicone compositioncomprising: a) from 50% to 95% (by weight, based on total polymer)organopolysiloxane polymer; b) from 1% to 10% (by weight, based onorganopolysiloxane) silicone functional crosslinker; and c) from 5% to50% (by weight, based on total polymer) dispersed organic polymer. 5.The curable silicone composition of claim 4 wherein the curable siliconecomposition comprises from 55% to 93% by weight organopilysiloxanepolymer.
 6. The curable silicone composition of claim 5 wherein thecurable silicone composition comprises from 57% to 91% by weightorganopilysiloxane polymer.
 7. The curable silicone composition of claim4 wherein the curable silicone composition comprises from 7% to 45% byweight organic polymer.
 8. The curable silicone composition of claim 7wherein the curable silicone composition comprises from 9% to 43% byweight organic polymer.
 9. The curable silicone composition of claim 4wherein the organopolysiloxane polymer has at least two reactivefunctional groups on the polymer chain.
 10. The curable silicone ofclaim 9 wherein the reactive functional groups are selected from thegroup consisting of hydroxyl, alkoxy, silicone alkoxy, acyloxy,ketoximo, amino, amido, aminoxy, alkenoxy, alkenyl, enoxy and mixturesthereof.
 11. The curable silicone composition of claim 10 wherein thereactive functional groups are end groups.
 12. The curable siliconecomposition of claim 4 wherein the organic polymer is selected from thegroup consisting of silylated polyurethane, non-silylated polyurethane,silylated allylic terminated polyether, a polyether that contains asilicone functional group, a silylated and non-silated acrylicfunctional polymer, a silylated and non-silated butyl functionalpolymer, and copolymers and mixtures thereof.
 13. The curable siliconecomposition of claim 12 wherein the elongation of the siliconecomposition, once cured, is at least 150%.
 14. The curable siliconecomposition of claim 13 wherein the curable silicone composition, oncecured, can be painted without the formation of fish eyes.
 15. Thecurable silicone composition of claim 4 wherein the curable siliconecomposition, once cured, passes a paint adhesion tape test.
 16. Acurable silicone composition comprising: a) from 50% to 95% (by weightbased on total polymer weight) organopolysiloxane polymer; b) from 1% to10% by weight silicone functional crosslinker; and c) an organic polymeror oligomer, wherein the organic polymer or oligomer is selected fromthe group consisting of silylated polyurethane, silylated allylicterminated polyether, polyether having a silicone functional group,silylated acrylic multipolymer, butyl functional polymer, andcombinations thereof; wherein the ranges of organic polymer (by weightbased on total polymer) are from 15% to 50% for silylated polyurethane;from 15% to 50% for non-silylated polyurethane; from 15% to 50% forsilylated allylic terminated polyether; from 15% to 50% silylatedallylic terminated acrylic polyether; from 15% to 50% for polyetherhaving a silicone functional group; from 10% to 50% for silylated andnon-silylated acrylic multipolymer; and from 5% to 50% for silylated andnon-silylated butyl functional polymer.
 17. The curable siliconecomposition of claim 16 wherein the organopolysiloxane has a molecularweight in the range from 20,000 to 100,000 grams/mole.
 18. The curablesilicone composition of claim 16 wherein the organopolysiloxane has atleast two reactive groups and an organic polymer selected from the groupconsisting of silylated polyurethane, non-silylated polyurethane,silylated allylic terminated polyether, a polyether that contains asilicone functional group, a silylated acrylic functional polymer, anon-silylated acrylic functional polymer, a silylated acrylic functionalpolymer, a non-silylated acrylic functional polymer, and mixturesthereof.
 19. The curable silicone composition of claim 18 wherein thereactive groups are selected from end groups, pendant groups, andcombinations thereof.
 20. The curable silicone composition of claim 16wherein the silicone crosslinker is selected from the group consistingof oximes, alkoxysilanes, epoxyalkylalkoxysilanes, amido silanes,aminosilanes, enoxysilanes, tetraethoxysilanes, methyltrimethoxysilane,vinyltrimethoxysilane, glycidoxypropyltrimethoxsilane,vinyltris-isopropenoxysilane, methyltris-isopropenoxysilane,methyltris-cyclohexylaminosilane, methyltris-secondarybutylaminosilane,condensation cure catalysts, and combinations thereof.
 21. The curablesilicone composition of claim 20 wherein the crosslinker is an oximecrosslinker.
 22. The curable silicone composition of claim 21 whereinthe oxime crosslinker is selected fromvinyltris-methylethylketoximosilane,methyltris-methylethylketoximosilane, and combinations thereof.
 23. Thecurable silicone composition of claim 16 wherein the siliconecomposition is selected from the group consisting of 1-part curablecompositions, 2-part curable compositions, and combinations thereof. 24.The curable silicone composition of claim 16 wherein thepolyorganosiloxane is selected from the group consisting of thermallycuring systems and room temperature curing systems.
 25. The curablesilicone composition of claim 16 wherein the composition comprises anextrusion or an in situ cured system.
 26. The curable siliconecomposition of claim 16 further comprising from 0.01% to 2% (by totalweight) catalyst.
 27. The curable silicone composition of claim 26wherein the catalyst is selected from the group consisting of metalsalts of carboxylic acids, organotitanates, platinum complexes,peroxides, and combinations thereof.
 28. The curable siliconecomposition of claim 27 wherein the catalyst comprises metal salts ofcarboxylic acids selected from the group consisting ofdibutyltindilaurate, dibutyltindiacetate,dimethyltindi-2-ethylhexanoate, and combinations thereof.
 29. Thecurable silicone composition of claim 27 wherein the catalyst comprisesorganotitanates selected from the group consisting oftetrabutyltitanate, tetra-n-propyltitanate,diisopropoxydi(ethoxyacetoacetyl)titanate,bis(acetylacetonyl)diisopropyl titanate and combinations thereof. 30.The curable silicone composition of claim 27 wherein the catalystcomprises a platinum complex.
 31. The curable silicone composition ofclaim 27 wherein the catalyst comprises a peroxide.
 32. The curablesilicone composition of claim 16 further comprising from 3% to 60% (bytotal weight) reinforcement agents, semi-reinforcing agents, orcombinations thereof.
 33. The curable silicone composition of claim 32wherein the reinforcement agent is selected from the group consisting ofhydrophobic treated fumed silicas, untreated fumed silicas, hydrophobicprecipitated calcium carbonates, ground calcium carbonates, talc, zincoxides, polyvinyl chloride powders, soft acrylic polymers andcombinations thereof.
 34. The curable silicone composition of claim 16further comprising from 0.5% to 2% (by total weight) adhesion promoter.35. The curable silicone composition of claim 16 wherein the tensileelongation, once cured, is at least 150%.
 36. The curable siliconecomposition of claim 35 wherein the tensile elongation, once cured is atleast 200%.
 37. The curable silicone composition of claim 36 wherein thetensile elongation, once cured is at least 800%.
 38. The curablesilicone composition of claim 16 wherein the organic polymer is asilylated polyurethane polymer, wherein the silylated polyurethanepolymer is derived by the steps of a) reacting a diisocyanate compoundwith a polyol to form an intermediate, wherein the intermediate isselected from isocyantates and hydroxyl terminated polyurethaneprepolymers; and b) silylating the intermediate.
 39. The curablesilicone composition of claim 38 wherein intermediate is silylated withan organo functional silane having one or more hydrolyzable groups. 40.The curable silicone composition of claim 39 wherein the hydrolyzablegroup is selected from the group consisting of (OCH₃)₃, (OCH₂CH₃)₃,oximo, enoxy, isopropenoxy,

and combinations thereof.
 41. The curable silicone composition of claim39 wherein the organo functional silane is of the formula:R″—X—Si—R′ wherein R′ is selected from the group consisting of (OCH₃)₃,(OCH₂CH₃)₃, CH₃(OCH₃)₂, or CH₃(OCH₂CH₃)₂, other hydrolyzable groups suchas oximo substituents, enoxy, and isopropenoxy; R″ is selected from thegroup consisting of amino, ureido, mercapto, isocyanato, and epoxy; andX is C₁ to C₈.
 42. The curable silicone composition of claim 38 whereinthe molecular weight of the polyurethane prepolymer intermediate rangesfrom 5,000 to 50,000 g/mol.
 43. The curable silicone composition ofclaim 38 wherein the polyurethane prepolymer intermediate has a NCO:OHratio in the range from 1.4:1 to 3:1 or an OH:NCO ratio in the rangefrom 1.4:1 to 3:1.
 44. The curable silicone composition of claim 16wherein organic polymer is a silylated allylic terminated polyether;wherein the silylated allylic terminated polyether is derived from thereaction of a vinyl alkyl terminated polyol with a hydride functionalsilane.
 45. The curable silicone composition of claim 44 wherein thehydride functional silane is selected from the group consisting oftriethoxysilane, trimethoxysilane, methyldiethoxysilane,methyldimethylsilane and combinations thereof.
 46. The curable siliconecomposition of claim 16 wherein the organic polymer is a polyetherhaving a silicone functional group.
 47. The curable silicone compositionof claim 46 wherein the silicone functional group is a hydrolyzablesilane group.
 48. The curable silicone composition of claim 46 whereinthe polyether having a silicone functional group has a molecular weightthat ranges from 2,000 to 50,000 g/mole.